共查询到17条相似文献,搜索用时 140 毫秒
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介绍了一种基于VC++6.0的表面等离体激元共振(SPR)生物传感检测系统软件的设计与实现.软件利用VC++6.0的MSComm控件,通过串口输入采集数据,结合Access数据库对数据进行操作、保存.数据处理后可得到SPR信号中的共振角度,并可实时绘制出反应曲线.同时,可以选择不同的化学反应动力学模式与相应的公式进行化学反应动力学的模拟,以便实验过程的指导和实验结果的分析.该软件已用于本实验室自主研制的Kretschman结构SPR生物传感器.水和空气的传感检测实验证实了该软件在SPR生物传感信号采集与分析中的可行性. 相似文献
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参比型SPR生物传感器是一种可以在单通道内实现对检测、参比两个位点同时检测的新型SPR分析系统.利用参比型SPR生物传感器在线制备了两种SARS病毒抗原的检测芯片.直接固定抗体法制备的检测芯片在检测时基本无反应;蛋白A固定抗体法制备的芯片在通入灭活SARS病毒时检测信号明显,参比信号略有上升.第二种芯片可以直接检测到病毒培养液上清中的灭活SARS病毒,检测灵敏度已达到1.66×104 PFU/mL.参比位点可以用来检测待测物中杂质引起的非特异性吸附. 相似文献
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介绍了一种采用不规则四边形棱镜设计的小型化表面等离子体共振(SPR)生物传感器。棱镜结构与已有的TI Spreeta传感器类似,但是在尺寸、光学性能等方面做了较大优化。新研制的SPR传感器在光学检测精度和系统集成性等方面也有了很大提高。在光路设计中,采用波长为630 nm的宽光束红光LED作为光源,5 000像素点线阵CCD作为光电检测器,光学检测效果要大大优于TI Spreeta波长为830 nm的近红外光源和128像素点的线阵硅光二极管。在光路优化的同时,系统集成了流动控制模块、信号采集处理模块,形成了一个可实现生物大分子相互作用分析的集成小型化SPR检测装置。利用空气、水及乙醇等进行的SPR实验表明:该装置能够对单一样本进行精确检测,共振角的检测精度高达0.01°,且检测结果线性度高,稳定性好,单一样本的检测偏差小于0.5%。 相似文献
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光纤表面等离体激元共振传感器是一种易于小型化的SPR传感器,常用于开发便携式传感检测设备,也可用于远距离实时在线检测.在本研究中,采用特制光纤作为导光介质来制作一种新的光纤SPR传感器.由于光纤中光传播相当复杂.仅凭过往经验来设计传感器将不能保证其检测精度.因此,针对本研究中光纤的特点,建立了光纤中光传播模型,并结合菲涅耳公式推导出该类光纤SPR传感器中光总反射系数与光波长的关系,最终绘制出理论SPR曲线并计算出共振波长.研究结果为该类光纤SPR传感器的设计及光谱分析提供了重要理论依据. 相似文献
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利用表面等离子体共振(SPR)生物传感技术,建立了一种可以快速准确分析血样中C反应蛋白的新方法。SPR传感器采用Kretschmann结构的角度连续扫描方式,使用2个步进电机分别驱动棱镜和光电检测器件转动进行单一样本的高精度分析。将C反应蛋白抗体修饰于敏感芯片表面,通过SPR传感器对血样中C反应蛋白浓度进行检测分析。利用SPR方法和传统免疫比浊法分别检测标准C反应蛋白样本和200份感染性疾病儿童患者(7~10岁,男112名,女88名)的血液样本,结果表明:SPR方法检测标准样本的线性变化区域更大。在患儿血样的检测中,尽管2种方法的结果基本相同,但是SPR检测速度更快,样本需求量更小、重复性更佳。这表明SPR生物传感分析方法在C反应蛋白检测中比传统方法更具优势,有望在临床检验分析中得以广泛应用。 相似文献
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Byoung-Jin JeonAuthor Vitae Moo-Hwan KimAuthor VitaeJae-Chul PyunAuthor Vitae 《Sensors and actuators. B, Chemical》2011,154(2):89-95
The surface plasmon resonance (SPR) biosensors have been used to detect various target analytes by using highly specific antigen-antibody interactions. In this work, a parylene film modified to have primary amine groups was applied as a linker layer of the SPR biosensor, and the primary amine groups were used for the covalent immobilization of proteins to the SPR biosensor. The feasibility of the parylene film as a linker layer was presented by estimating the influence of the parylene film on the SPR measurement parameters, such as the sensitivity and the detection range. Then, a model protein called horseradish peroxidase (HRP) was used to demonstrate the improved immobilization efficiency as well as the sensitivity of the SPR biosensor with the parylene-A film. Additionally, a reconstruction method of the immunoaffinity layer was presented by using oxygen plasma. 相似文献
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Qing WangAuthor VitaeJiahao HuangAuthor Vitae Xiaohai YangAuthor VitaeKemin WangAuthor Vitae Leiliang HeAuthor VitaeXiaoping LiAuthor Vitae Caoye XueAuthor Vitae 《Sensors and actuators. B, Chemical》2011,156(2):893-898
It was difficult to detect small molecules directly using conventional surface plasmon resonance (SPR) biosensors since the changes of refractive index, which was resulted by binding small molecules, were usually small. In this paper, split aptamer fragments were used for the construction of SPR biosensor to determine small molecule such as adenosine with high sensitivity. An aptamer for adenosine was designed to be two flexible ssDNA pieces, one was tethered on Au film and the other was modified on Au nanoparticles (AuNPs). In the presence of adenosine, two ssDNA pieces reassembled into the intact aptamer structure and the AuNPs-labeled adenosine-aptamer complex was formed on the Au film. Then, the resonance wavelength shift was enhanced obviously, due to the electronic coupling between the localized plasmon of AuNPs and the surface plasmon wave associated with Au film. The results confirmed that this biosensor could detect adenosine with high sensitivity and selectivity. The limitation of detection (LOD) of this SPR biosensor was ca. 1.5 pM, which was an approximately ca. 2-3 order of magnitude lower than that of those SPR biosensors which utilized competitive methods. 相似文献
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表面等离子体共振 (SPR)技术是一种简单直接的传感技术 ,SPR对金属表面附近的折射率的变化极为敏感 ,利用这一性质 ,表面等离子体共振传感器已成为生物传感器研究领域的热点。现提出一种电光调制波导型SPR模型 ,模拟计算表明该模型在不损害灵敏度的条件下 ,扩大了探测的动态范围。 相似文献
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A surface plasmon resonance (SPR) biosensor was used to determine the recombinant group 1 house dust mite allergen (rDer f1) in both HBS-EP buffer and fetal bovine serum (FBS). The monoclonal antibody was immobilized onto the CM5 sensor chip surface using an amine coupling method. The procedures of antibody immobilization and the subsequent primary and enhanced immunoassay were monitored in real time. The sensitivity for rDer f1 detection was remarkably improved by using intact polyclonal antibody as signal amplifying agent. Using this signal enhanced SPR immunosensor, rDer f1 in HBS-EP buffer and FBS was detected at a concentration of 15.4 and 32.1 ng/ml, respectively. The result demonstrates that SPR biosensor is a simple and reliable method for allergen detection. 相似文献